The epidermolytic (exfoliative) toxins of Staphylococcus aureus

Two epidermolytic toxins, produced by different strains of Staphylococcus aureus, split human skin at a site in the upper epidermis. Clinical effects are most common in infants, but adults are susceptible. Epidermolysis may also be observed in the mouse, in vivo and in vitro, and in a few other mamm...

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Bibliographic Details
Published in:Medical microbiology and immunology 1995-08, Vol.184 (2), p.53-61
Main Authors: BAILEY, C. J, LOCKHART, B. P, REDPATH, M. B, SMITH, T. P
Format: Article
Language:English
Subjects:
Animals
Bacteriology
Biological and medical sciences
Endopeptidases - toxicity
Exfoliatins - chemistry
Exfoliatins - genetics
Exfoliatins - toxicity
Fundamental and applied biological sciences. Psychology
Humans
Mice
Microbiology
Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains
Skin - drug effects
Staphylococcus aureus - pathogenicity
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Summary:Two epidermolytic toxins, produced by different strains of Staphylococcus aureus, split human skin at a site in the upper epidermis. Clinical effects are most common in infants, but adults are susceptible. Epidermolysis may also be observed in the mouse, in vivo and in vitro, and in a few other mammals. Recent in vitro experiments have demonstrated an inhibition by chelators and point to metal-ion, possibly Ca2+, involvement. The epidermolysis effect is insensitive to a wide range of other metabolic inhibitors. The toxin amino acid sequences are similar to that of staphylococcal proteinase, and new experiments by chemical modification and site-directed mutagenesis have shown that toxicity depends on 'active serine' residues of a catalytic triad similar to that found in serine proteases. Furthermore the toxins possess esterolytic activity, also dependent on the 'active serine' sites. However, the toxins have low or undetectable activity towards a range of peptide or protein substrates. In histological and related studies, the toxins bound selectively to an intracellular skin protein, profilaggrin, but there was no evidence that the toxin can enter intact epidermal cells. Therefore, although the circumstantial evidence that the toxins act by proteolysis is convincing, a specific skin proteolytic substrate for the toxin has not been identified.
ISSN:0300-8584
1432-1831
DOI:10.1007/BF00221387